Canonical Allele Identifier: CA15710492

Gene: HTR3B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113946934T>A , CM000673.2:g.113946934T>A	GRCh38
NC_000011.9:g.113817656T>A , CM000673.1:g.113817656T>A	GRCh37
NC_000011.8:g.113322866T>A	NCBI36
NG_011483.1:g.47068T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.*797T>A MANE Select	ENSP00000260191.2:n.*797T>A
ENST00000260191.7:c.*797T>A	ENSP00000260191.2:n.*797T>A
XM_017018552.2:c.*797T>A	XP_016874041.1:n.*797T>A
XR_001748034.2:n.2163T>A
NM_001363563.2:c.*797T>A	NP_001350492.1:n.*797T>A
NM_006028.5:c.*797T>A MANE Select	NP_006019.1:n.*797T>A